Nephroplex

Product NDC
43857-0136
11-digit product format
438570136
Labeler code
43857
Product ID
43857-0136_fd6b4539-44c5-414d-8134-1ba1f7c12053
Type
HUMAN OTC DRUG
Nonproprietary name
Berberis Vulgaris, Hydrangea Arborescens, Petroselinum Sativum, Solidago Virgaurea, Uva Ursi, Rubia Tinctorum, Glutathione, Kidney (Suis), Bryonia (Alba), Eupatorium Purpureum, Mercurius Corrosivus
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-01-14
Substance
ARCTOSTAPHYLOS UVA-URSI LEAF; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; EUTROCHIUM PURPUREUM ROOT; GLUTATHIONE; HYDRANGEA ARBORESCENS ROOT; MERCURIC CHLORIDE; PETROSELINUM CRISPUM; PORK KIDNEY; RUBIA TINCTORUM ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP
Active strength
3; 3; 12; 12; 6; 3; 12; 3; 6; 5; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
3M5V3D1X36ARCTOSTAPHYLOS UVA-URSI LEAFARCTOSTAPHYLOS UVA-URSI LEAF
1TH8Q20J0UBERBERIS VULGARIS ROOT BARKBERBERIS VULGARIS ROOT BARK
T7J046YI2BBRYONIA ALBA ROOTBRYONIA ALBA ROOT
0VYG5PVN5QEUTROCHIUM PURPUREUM ROOTEUTROCHIUM PURPUREUM ROOT
GAN16C9B8OGLUTATHIONE70-18-8GLUTATHIONE
SFK828Q2DEHYDRANGEA ARBORESCENS ROOTHYDRANGEA ARBORESCENS ROOT
53GH7MZT1RMERCURIC CHLORIDE7487-94-7MERCURIC CHLORIDE
1WZA4Y92EXPETROSELINUM CRISPUMPETROSELINUM CRISPUM
X7BCI5P86HPORK KIDNEYPORK KIDNEY
0SVP95L23GRUBIA TINCTORUM ROOTRUBIA TINCTORUM ROOT
5405K23S50SOLIDAGO VIRGAUREA FLOWERING TOPSOLIDAGO VIRGAUREA FLOWERING TOP

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0136-14385701360130 mL in 1 BOTTLE, DROPPER (43857-0136-1) 30 ml2016-09-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug Facts:BioActive Nutritional, Inc. | Apotheca Company2016-09-13HUMAN OTC DRUG LABEL2